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Showing results (151-160 of 167) with videos related to

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Frontiers in Pediatrics|July 11, 2022
First Identification of Rare Exonic and Deep Intronic Splice-Altering Variants in Patients With Beta-SarcoglycanopathyZhiying Xie, Chengyue Sun, Chang Liu, et al.
Journal of Medical Genetics|September 30, 2020
Molecular landscape of CAPN3 mutations in limb-girdle muscular dystrophy type R1: from a Chinese multicentre analysis to a worldwide perspectiveHuahua Zhong, Yiming Zheng, Zhe Zhao, et al.
Journal of Thrombosis and Thrombolysis|October 22, 2021
Antithrombotic strategy and its relationship with outcomes in patients with atrial fibrillation and chronic coronary syndromeWen-He Lv, Jian-Zeng Dong, Xin Du, et al.
Frontiers in Molecular Neuroscience|October 31, 2022
Clinical and biochemical characterization of hereditary transthyretin amyloidosis caused by E61K mutationXujun Chu, Mengdie Wang, Ran Tang, et al.
American Journal of Human Genetics|February 12, 2022
The CGG repeat expansion in RILPL1 is associated with oculopharyngodistal myopathy type 4Jiaxi Yu, Jingli Shan, Meng Yu, et al.
Nano Letters|September 15, 2025
Revealing Nanoscale Inhomogeneities in a Superconducting Nanowire through Self-Heating Hotspot Scanning and MappingZhen Liu, Qing-Yuan Zhao, Hao Hao, et al.
Annals of Clinical and Translational Neurology|May 4, 2021
GGC repeat expansions in NOTCH2NLC causing a phenotype of distal motor neuropathy and myopathyJiaxi Yu, Xing-Hua Luan, Meng Yu, et al.
Brain : a Journal of Neurology|March 11, 2021
The GGC repeat expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy type 3Jiaxi Yu, Jianwen Deng, Xueyu Guo, et al.
Pacing and Clinical Electrophysiology : PACE|February 26, 2024
Catheter ablation of atrial fibrillation in patients with left bundle branch blockRi-Bo Tang, Wen-He Lv, De-Yong Long, et al.
Nature Chemical Biology|January 12, 2023
Small molecule agonist of mitochondrial fusion repairs mitochondrial dysfunctionYingjie Guo, Huan Zhang, Chen Yan, et al.
Pageof 17

Showing results (151-160 of 167) with videos related to

Sort By:
Pageof 17
Frontiers in Pediatrics|July 11, 2022
First Identification of Rare Exonic and Deep Intronic Splice-Altering Variants in Patients With Beta-SarcoglycanopathyZhiying Xie, Chengyue Sun, Chang Liu, et al.
Journal of Medical Genetics|September 30, 2020
Molecular landscape of CAPN3 mutations in limb-girdle muscular dystrophy type R1: from a Chinese multicentre analysis to a worldwide perspectiveHuahua Zhong, Yiming Zheng, Zhe Zhao, et al.
Journal of Thrombosis and Thrombolysis|October 22, 2021
Antithrombotic strategy and its relationship with outcomes in patients with atrial fibrillation and chronic coronary syndromeWen-He Lv, Jian-Zeng Dong, Xin Du, et al.
Frontiers in Molecular Neuroscience|October 31, 2022
Clinical and biochemical characterization of hereditary transthyretin amyloidosis caused by E61K mutationXujun Chu, Mengdie Wang, Ran Tang, et al.
American Journal of Human Genetics|February 12, 2022
The CGG repeat expansion in RILPL1 is associated with oculopharyngodistal myopathy type 4Jiaxi Yu, Jingli Shan, Meng Yu, et al.
Nano Letters|September 15, 2025
Revealing Nanoscale Inhomogeneities in a Superconducting Nanowire through Self-Heating Hotspot Scanning and MappingZhen Liu, Qing-Yuan Zhao, Hao Hao, et al.
Annals of Clinical and Translational Neurology|May 4, 2021
GGC repeat expansions in NOTCH2NLC causing a phenotype of distal motor neuropathy and myopathyJiaxi Yu, Xing-Hua Luan, Meng Yu, et al.
Brain : a Journal of Neurology|March 11, 2021
The GGC repeat expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy type 3Jiaxi Yu, Jianwen Deng, Xueyu Guo, et al.
Pacing and Clinical Electrophysiology : PACE|February 26, 2024
Catheter ablation of atrial fibrillation in patients with left bundle branch blockRi-Bo Tang, Wen-He Lv, De-Yong Long, et al.
Nature Chemical Biology|January 12, 2023
Small molecule agonist of mitochondrial fusion repairs mitochondrial dysfunctionYingjie Guo, Huan Zhang, Chen Yan, et al.
Pageof 17